meddevicedb.com FDA Device Reference

DRUG DISPENSING SPIKE

K946190 Class II Traditional
Decision Date
1995-03-17
Sponsor / Applicant
Gelman Sciences, Inc.

Technical Specification

510(k) Submission ID K946190
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1995-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRUG DISPENSING SPIKE received FDA 510(k) clearance under submission number K946190, sponsored by Gelman Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1995-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.